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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Poly(GR) impairs protein translation and stress granule dynamics in C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis
Yong‐Jie Zhang, Tania F. Gendron, Mark Ebbert, et al.
Nature Medicine (2018) Vol. 24, Iss. 8, pp. 1136-1142
Open Access | Times Cited: 288

Showing 26-50 of 288 citing articles:

G4C2 Repeat RNA Initiates a POM121-Mediated Reduction in Specific Nucleoporins in C9orf72 ALS/FTD
Alyssa N. Coyne, Benjamin L. Zaepfel, Lindsey R. Hayes, et al.
Neuron (2020) Vol. 107, Iss. 6, pp. 1124-1140.e11
Open Access | Times Cited: 132
CRISPR-Cas9 Screens Identify the RNA Helicase DDX3X as a Repressor of C9ORF72 (GGGGCC)n Repeat-Associated Non-AUG Translation
Weiwei Cheng, ShaoPeng Wang, Zhe Zhang, et al.
Neuron (2019) Vol. 104, Iss. 5, pp. 885-898.e8
Open Access | Times Cited: 127
Genetic Convergence Brings Clarity to the Enigmatic Red Line in ALS
Casey Cook, Leonard Petrucelli
Neuron (2019) Vol. 101, Iss. 6, pp. 1057-1069
Open Access | Times Cited: 125
Reduced autophagy upon C9ORF72 loss synergizes with dipeptide repeat protein toxicity in G4C2 repeat expansion disorders
Manon Boivin, Véronique Pfister, Angéline Gaucherot, et al.
The EMBO Journal (2020) Vol. 39, Iss. 4
Open Access | Times Cited: 120
C9orf72 arginine-rich dipeptide repeat proteins disrupt karyopherin-mediated nuclear import
Lindsey R. Hayes, Lauren Duan, Kelly Bowen, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 119
Long-read sequencing across the C9orf72 ‘GGGGCC’ repeat expansion: implications for clinical use and genetic discovery efforts in human disease
Mark Ebbert, Stefan L. Farrugia, Jonathon Sens, et al.
Molecular Neurodegeneration (2018) Vol. 13, Iss. 1
Open Access | Times Cited: 114
C9orf72 arginine-rich dipeptide proteins interact with ribosomal proteins in vivo to induce a toxic translational arrest that is rescued by eIF1A
Thomas G. Moens, Teresa Niccoli, Katherine Wilson, et al.
Acta Neuropathologica (2019) Vol. 137, Iss. 3, pp. 487-500
Open Access | Times Cited: 111
Physiological, Pathological, and Targetable Membraneless Organelles in Neurons
Veronica H. Ryan, Nicolas L. Fawzi
Trends in Neurosciences (2019) Vol. 42, Iss. 10, pp. 693-708
Open Access | Times Cited: 105
Nuclear accumulation of CHMP7 initiates nuclear pore complex injury and subsequent TDP-43 dysfunction in sporadic and familial ALS
Alyssa N. Coyne, Victoria Baskerville, Benjamin L. Zaepfel, et al.
Science Translational Medicine (2021) Vol. 13, Iss. 604
Open Access | Times Cited: 102
Nuclear Import Receptors Directly Bind to Arginine-Rich Dipeptide Repeat Proteins and Suppress Their Pathological Interactions
Saskia Hutten, Sinem Usluer, Benjamin Bourgeois, et al.
Cell Reports (2020) Vol. 33, Iss. 12, pp. 108538-108538
Open Access | Times Cited: 99
Motor dysfunction and neurodegeneration in a C9orf72 mouse line expressing poly-PR
Zongbing Hao, Liu Liu, Zhouteng Tao, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 80
New pathologic mechanisms in nucleotide repeat expansion disorders
Caitlin M. Rodriguez, Peter K. Todd
Neurobiology of Disease (2019) Vol. 130, pp. 104515-104515
Open Access | Times Cited: 77
Ribosome inhibition by C9ORF72-ALS/FTD-associated poly-PR and poly-GR proteins revealed by cryo-EM
A.B. Loveland, E. Svidritskiy, Denis Susorov, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 62
Huntington’s disease mice and human brain tissue exhibit increased G3BP1 granules and TDP43 mislocalization
Isabella Sanchez, Thai B. Nguyen, Whitney England, et al.
Journal of Clinical Investigation (2021) Vol. 131, Iss. 12
Open Access | Times Cited: 57
NUP62 localizes to ALS/FTLD pathological assemblies and contributes to TDP-43 insolubility
Amanda M. Gleixner, Brandie Morris Verdone, Charlton G. Otte, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 51
CRISPR/Cas9-mediated excision of ALS/FTD-causing hexanucleotide repeat expansion in C9ORF72 rescues major disease mechanisms in vivo and in vitro
Katharina E. Meijboom, Abbas Abdallah, Nicholas P. Fordham, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 42
Biological importance of arginine: A comprehensive review of the roles in structure, disorder, and functionality of peptides and proteins
Munishwar N. Gupta, Vladimir N. Uversky
International Journal of Biological Macromolecules (2023) Vol. 257, pp. 128646-128646
Open Access | Times Cited: 35
Microglia and Astrocytes in Amyotrophic Lateral Sclerosis: Disease-Associated States, Pathological Roles, and Therapeutic Potential
Justin You, Mohieldin Youssef, Jhune Rizsan Santos, et al.
Biology (2023) Vol. 12, Iss. 10, pp. 1307-1307
Open Access | Times Cited: 24
PolyGR and polyPR knock-in mice reveal a conserved neuroprotective extracellular matrix signature in C9orf72 ALS/FTD neurons
Carmelo Milioto, Mireia Carcolé, Ashling Giblin, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 4, pp. 643-655
Open Access | Times Cited: 15
Friend or foe: The role of stress granule in neurodegenerative disease
Qinqin Cui, Zhongyi Liu, Ge Bai
Neuron (2024) Vol. 112, Iss. 15, pp. 2464-2485
Closed Access | Times Cited: 15
Antisense Oligonucleotides (ASOs) in Motor Neuron Diseases: A Road to Cure in Light and Shade
Silvia Cantara, Giorgia Simoncelli, Claudia Ricci
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 9, pp. 4809-4809
Open Access | Times Cited: 12
NLS-binding deficient Kapβ2 reduces neurotoxicity via selective interaction with C9orf72-ALS/FTD dipeptide repeats
Kevin M. Kim, Amandeep Girdhar, M.E. Cicardi, et al.
Communications Biology (2025) Vol. 8, Iss. 1
Open Access | Times Cited: 1
CASP8 intronic expansion identified by poly-glycine-arginine pathology increases Alzheimer’s disease risk
Lien Nguyen, Ramadan Ajredini, Shu Guo, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 7
Open Access | Times Cited: 1
PTPσ-mediated PI3P regulation modulates neurodegeneration in C9ORF72-ALS/FTD
Zhe Zhang, Xiujuan Fu, Noelle Wright, et al.
Neuron (2025)
Closed Access | Times Cited: 1
Nucleocytoplasmic transport defects in neurodegeneration — Cause or consequence?
Saskia Hutten, Dorothee Dormann
Seminars in Cell and Developmental Biology (2019) Vol. 99, pp. 151-162
Closed Access | Times Cited: 76

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